Matrilins mediate weak cell attachment without promoting focal adhesion formation

被引:16
作者
Mann, Henning H.
Sengle, Gerhard
Gebauer, Jan M.
Eble, Johannes A.
Paulsson, Mats
Wagener, Raimund
机构
[1] Univ Cologne, Fac Med, Ctr Biochem, D-50931 Cologne, Germany
[2] Univ Hosp Munster, Inst Physiol Chem & Pathobiochem, D-48129 Munster, Germany
[3] Univ Cologne, Fac Med, Ctr Mol Med, D-50931 Cologne, Germany
关键词
matrilin; integrin; heparan sulfate proteoglycan; cell attachment; cell spreading;
D O I
10.1016/j.matbio.2006.10.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The matrilins form a family of non-collagenous adaptor proteins in the extracellular matrix. The extracellular ligand interactions of matrilins have been studied in some detail, while the potential interplay between matrilins and cells has been largely neglected. Except for matrilin-4, all matrilins mediate cell attachment, but only for matrilin-1 and -3 the binding is clearly dose dependent and seen already at moderate coating concentrations. Even so, much higher concentrations of matrilin-1 or -3 than of fibronectin are required for cell attachment to reach plateau values. Integrins contribute to the matrilin-mediated cell attachment, but the binding does not lead to formation of focal contacts and reorganisation of the actin cytoskeleton. Cells deficient in beta 1 integrins are able to adhere, although weaker, and matrilins do not bind the soluble integrin alpha 1 beta 1 and alpha 2 beta 1 ectodomains. Cell surface proteoglycans may promote the attachment, as cells deficient in glycosaminoglycan biosynthesis adhere less well to matrilin-3. Even so, exogenous glycosaminoglycans are not able to compete for the attachment of HaCaT cells to matrilins. (c) 2006 Elsevier B.V./International Society of Matrix Biology. All rights reserved.
引用
收藏
页码:167 / 174
页数:8
相关论文
共 36 条
  • [1] Adamczyk John J. Jr., 2001, Journal of Insect Science (Tucson), V1, P1
  • [2] Cell-matrix contact structures
    Adams, JC
    [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 2001, 58 (03) : 371 - 392
  • [3] MONOCLONAL-ANTIBODY 9EG7 DEFINES A NOVEL BETA(1) INTEGRIN EPITOPE INDUCED BY SOLUBLE LIGAND AND MANGANESE, BUT INHIBITED BY CALCIUM
    BAZZONI, G
    SHIH, DT
    BUCK, CA
    HEMLER, ME
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (43) : 25570 - 25577
  • [4] BJORNSSON S, 1981, BIOCHEM J, V198, P141
  • [5] NORMAL KERATINIZATION IN A SPONTANEOUSLY IMMORTALIZED ANEUPLOID HUMAN KERATINOCYTE CELL-LINE
    BOUKAMP, P
    PETRUSSEVSKA, RT
    BREITKREUTZ, D
    HORNUNG, J
    MARKHAM, A
    FUSENIG, NE
    [J]. JOURNAL OF CELL BIOLOGY, 1988, 106 (03) : 761 - 771
  • [6] Pseudoachondroplasia and multiple epiphyseal dysplasia: Mutation review, molecular interactions, and genotype to phenotype correlations
    Briggs, MD
    Chapman, KL
    [J]. HUMAN MUTATION, 2002, 19 (05) : 465 - 478
  • [7] Altered integration of matrilin-3 into cartilage extracellular matrix in the absence of collagen IX
    Budde, B
    Blumbach, K
    Ylöstalo, J
    Zaucke, F
    Ehlen, HWA
    Wagener, R
    Ala-Kokko, L
    Paulsson, M
    Bruckner, P
    Grässel, S
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (23) : 10465 - 10478
  • [8] CARTILAGE MATRIX PROTEIN FORMS A TYPE-II COLLAGEN-INDEPENDENT FILAMENTOUS NETWORK - ANALYSIS IN PRIMARY-CELL CULTURES WITH A RETROVIRUS EXPRESSION SYSTEM
    CHEN, Q
    JOHNSON, DM
    HAUDENSCHILD, DR
    TONDRAVI, MM
    GOETINCK, PF
    [J]. MOLECULAR BIOLOGY OF THE CELL, 1995, 6 (12) : 1743 - 1753
  • [9] Assembly of a novel cartilage matrix protein filamentous network: Molecular basis of differential requirement of von Willebrand factor A domains
    Chen, Q
    Zhang, Y
    Johnson, DM
    Goetinck, PF
    [J]. MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (07) : 2149 - 2162
  • [10] Couchman JR, 1999, J CELL SCI, V112, P3415